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Familial partial lipodystrophy due to the LMNA R482W mutation with multinodular goitre, extrapyramidal syndrome and primary hyperaldosteronism

✍ Scribed by M. C. Vantyghem; F. Faivre-Defrance; S. Marcelli-Tourvieille; C. Fermon; A. Evrard; M. F. Bourdelle-Hego; C. Vigouroux; L. Defebvre; B. Delemer; J. L. Wemeau


Book ID
108703758
Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
85 KB
Volume
67
Category
Article
ISSN
0300-0664

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